NDC 50090-5705
Escitalopram 10 mg tablet
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-135.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · relabels it
Recalls
- Mar 24, 2016 · Class III · Lupin Limited
Labeling: Incorrect or Missing Lot and/or Expiration Date
Lots: Lot # G510086; Exp. 11/17
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Escitalopram: every company that makes it
- Form
- tablet
- Strength
- 10 mg
- Approval
- ANDA ANDA078169
- On the market since
- Sep 10, 2012
- Package NDCs
50090-5705-0- Official label
- DailyMed (National Library of Medicine), updated Oct 26, 2021
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